Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

From hydrodynamic equations

If these assumptions are satisfied then the ideas developed earlier about the mean free path can be used to provide qualitative but useful estimates of the transport properties of a dilute gas. While many varied and complicated processes can take place in fluid systems, such as turbulent flow, pattern fonnation, and so on, the principles on which these flows are analysed are remarkably simple. The description of both simple and complicated flows m fluids is based on five hydrodynamic equations, die Navier-Stokes equations. These equations, in trim, are based upon the mechanical laws of conservation of particles, momentum and energy in a fluid, together with a set of phenomenological equations, such as Fourier s law of themial conduction and Newton s law of fluid friction. When these phenomenological laws are used in combination with the conservation equations, one obtains the Navier-Stokes equations. Our goal here is to derive the phenomenological laws from elementary mean free path considerations, and to obtain estimates of the associated transport coefficients. Flere we will consider themial conduction and viscous flow as examples. [Pg.671]

The function / incorporates the screening effect of the surfactant, and is the surfactant density. The exponent x can be derived from the observation that the total interface area at late times should be proportional to p. In two dimensions, this implies R t) oc 1/ps and hence x = /n. The scaling form (20) was found to describe consistently data from Langevin simulations of systems with conserved order parameter (with n = 1/3) [217], systems which evolve according to hydrodynamic equations (with n = 1/2) [218], and also data from molecular dynamics of a microscopic off-lattice model (with n= 1/2) [155]. The data collapse has not been quite as good in Langevin simulations which include thermal noise [218]. [Pg.667]

From various studies" " it is becoming clear that in spite of a heat flux, the overriding parameter is the temperature at the interface between the metal electrode and the solution, which has an effect on diffusion coefficients and viscosity. If the variations of these parameters with temperature are known, then / l (and ) can be calculated from the hydrodynamic equations. [Pg.327]

In gridpoint models, transport processes such as speed and direction of wind and ocean currents, and turbulent diffusivities (see Section 4.8.1) normally have to be prescribed. Information on these physical quantities may come from observations or from other (dynamic) models, which calculate the flow patterns from basic hydrodynamic equations. Tracer transport models, in which the transport processes are prescribed in this way, are often referred to as off-line models. An on-line model, on the other hand, is one where the tracers have been incorporated directly into a d3mamic model such that the tracer concentrations and the motions are calculated simultaneously. A major advantage of an on-line model is that feedbacks of the tracer on the energy balance can be described... [Pg.75]

The results presented here are quite remarkable. The theory underlying derivation of the hydrodynamic equations assumes that all gradients and forces acting on the fluid are small. The MD fluids are under the influence of extremely large gradients and forces. Yet, we find results which are in both qualitative and quantitative agreement with macroscopic predictions. The appearance of spatial structure on such a small scale (10 cm) provides strong indications that fluid dynamics can be understood from a microscopic viewpoint. [Pg.251]

In addition to the fact that MPC dynamics is both simple and efficient to simulate, one of its main advantages is that the transport properties that characterize the behavior of the macroscopic laws may be computed. Furthermore, the macroscopic evolution equations can be derived from the full phase space Markov chain formulation. Such derivations have been carried out to obtain the full set of hydrodynamic equations for a one-component fluid [15, 18] and the reaction-diffusion equation for a reacting mixture [17]. In order to simplify the presentation and yet illustrate the methods that are used to carry out such derivations, we restrict our considerations to the simpler case of the derivation of the diffusion equation for a test particle in the fluid. The methods used to derive this equation and obtain the autocorrelation function expression for the diffusion coefficient are easily generalized to the full set of hydrodynamic equations. [Pg.99]

The hydrodynamic equations can be derived from the MPC Markov chain dynamics using projection operator methods analogous to those used to obtain... [Pg.104]

Here 0 is the Heaviside function. The projection operator formalism must be carried out in matrix from and in this connection it is useful to define the orthogonal set of variables, k,uk,5k > where the entropy density is sk = ek — CvTrik with Cv the specific heat. In terms of these variables the linearized hydrodynamic equations take the form... [Pg.105]

Since MPC dynamics yields the hydrodynamic equations on long distance and time scales, it provides a mesoscopic simulation algorithm for investigation of fluid flow that complements other mesoscopic methods. Since it is a particle-based scheme it incorporates fluctuations, which are essential in many applications. For macroscopic fluid flow averaging is required to obtain the deterministic flow fields. In spite of the additional averaging that is required the method has the advantage that it is numerically stable, does not suffer from lattice artifacts in the structure of the Navier-Stokes equations, and boundary conditions are easily implemented. [Pg.107]

With the surface-velocity expression known from the hydrodynamics, Equation 2 can be rewritten as... [Pg.486]

The earliest and simplest approach in this direction starts from Langevin equations with solutions comprising a spectrum of relaxation modes [1-4], Special features are the incorporation of entropic forces (Rouse model, [6]) which relax fluctuations of reduced entropy, and of hydrodynamic interactions (Zimm model, [7]) which couple segmental motions via long-range backflow fields in polymer solutions, and the inclusion of topological constraints or entanglements (reptation or tube model, [8-10]) which are mutually imposed within a dense ensemble of chains. [Pg.3]

Although trajectories are not computed in QFD-DFT, it is clear that there is a strong connection between this approach and the trajectory or hydrodynamical picture of quantum mechanics [20], independently developed by Madelung [21], de Broglie [22], and Bohm [23], which is also known as Bohmian mechanics. From the same hydrodynamical equations, information not only about the system... [Pg.106]

Of course, as was shown in Section V-A, this latter expression may also be derived starting from the hydrodynamical equations for the pair distribution and the Poisson equation it is also the final result of the theories developed independently by Falken-hagen and Ebeling,9 and by Friedman 12-13 in these two approaches, the starting point is a Liouville equation for the system of ions with an ad hoc stochastic term describing the interactions with the solvent. [Pg.253]

Cook equation of state, using covolume approximation) 63-4 (Other coyolume equations of state) 65 (Jones, Jones-Miller and Lennard-Jones equations of state) 66 (Cot-trell-Paterson equation of state) 12aj) W. Fickett W.W. Wood, Physics of Fluids 1, 528(1958 (A Detonation-Product Equation of State Observed from Hydrodynamic Data)... [Pg.297]

H) W. Fickett W.W. Wood, The Physics of Fluids 1 (6), 528-34 (Nov-Dec 1958) (Detonation-product equations of state, known as "constant-/ and "constant-)/ , obtained from hydrodynamic data) I) J.J. Erpenbeck D.G. Miller, IEC 51, 329-31 (March 1959) (Semiempirical vapor pressure relation based on Dieterici s equation of state J) K.A. Kobe P.S. Murti, IEC 51, 332 (March 1959) (Ideal critical volumes for generalized correlations) (Application to the Macleod equation of state) Kj) S. Katz et al, jApplPhys 10, 568-76(April 1959) (Hugoniot equation of state of aluminum and steel) K2) S.J. Jacobs, jAmRocketSoc 30, 151(1960) (Review of semi-empirical equations of state)... [Pg.298]

Detonation - Product Equation of State Obtained from Hydrodynamic Data is discussed by W. Fickett W.W. Wood in the Physics of Fluids 1, 528-34(1958)... [Pg.495]

Accdg to Dunkle (Ref 28), Brode (Ref 14), in order to solve detonation problems without recourse to empirical values derived from explosion measurements, integrated the hydrodynamical equations of motion (which constitute a set of nonlinear partial... [Pg.551]

A new relationship in the hydrodynamic theory of expl waves) 95) W.W. Wood J.G. Kirkwood, JChemPhys 29, 956(1958) (Present status of deton theory) 95a) W. Fickett 8t W.W. Wood, Phys of Fluids 1 (6), 528-34 (Nov-Dec. 1958) (A detonation-product equation of state obtained from hydrodynamic data) 96) Cook... [Pg.617]

The Maxwell theory is well known to be a material fluid flow theory [6],4 since the equations are hydrodynamic equations. In principle, anything that can be done with fluid theory can be done with electrodynamics, since the fundamental equations are the same mathematics and must describe consistent analogous functional behavior and phenomena [5]. This means that EM systems with electromagnetic energy winds from their active external atmosphere ... [Pg.702]

Detonation-product equation of state obtained from hydrodynamic data 4 D49S... [Pg.542]

In closing this section, we note that the stochastic master equation, Eq. (16), can be used to study the effect of boundary conditions on transport equations. If a(x, y, t) is sufficiently peaked as a function of x — y, that is if transitions occur from y to states in the near neighborhood of y, only, then the master equation can be approximated by a Fokker-Planck equation. The effects of the boundary on the master equation all appear in the properties of a(x, y, t). However, in the transition to the Fokker-Planck differential equation, these boundary effects appear as boundary conditions on the differential equation.7 These effects are prototypes for the study of how molecular boundary conditions imposed on the Liouville equation are reflected in the macroscopic boundary conditions imposed on the hydrodynamic equations. [Pg.8]

Understanding the order of the hydrodynamics equations, continuity and momentum, can be somewhat confusing and possibly not the same from problem to problem. The continuity and momentum equations must be viewed as a closely coupled system. Again, it is clear that the momentum equations are second order in velocity and first order in pressure. The continuity equation is first order in density. However, an equation of state requires that density be a function of pressure, and vice versa. Density and pressure must be dependent on each other through an algebraic equation. Therefore a substitution could be done to eliminate either pressure or density. As a result the coupled system is third order, which can present some practical issues for boundary-condition assignment. The first-order behavior must carry information from some portions of the boundary into the domain, but it does not communicate information back. Therefore, over some portions of a problem... [Pg.130]

The study of rotating disk electrode behavior provides a unique opportunity to develop a model that predicts the effect of diffusion and convection on the current. This is one of the few convective systems that have simple hydrodynamic equations that may be combined with the diffusion model developed herein to produce meaningful results. The effect of diffusion is modeled exactly as it has been done previously. The effect of convection is treated by integrating an approximate velocity equation to determine the extent of convective flow during a given At interval. Matter, then, is simply transferred from volume element to volume element in accord with this result to simulate convection. The whole process repeated results in a steady-state concentration profile and a steady-state representation of the current (the Levich equation). [Pg.613]

Amperometric detectors can operate over a range of conversion efficiencies from nearly 0% to nearly 100%. From a mathematical point of view, a classical amperometric determination (conversion of analyte is negligible) is one where the current output is dependent on the cube root of the linear velocity across the electrode surface as described by Levich s hydrodynamic equations for laminar flow. Conversely, the current response for a cell with 100% conversion is directly proportional to the velocity of the flowing solution. While the mathematics describing intermediate cases is quite interesting, it is beyond the scope of this chapter. [Pg.821]

The expression of the transverse current autocorrelation function can also be derived from the linearized hydrodynamic equations. Because it is decoupled from all the longitudinal modes, the derivation is simple and the final expression in wavenumber and Laplace frequency plane can be written as... [Pg.75]

This functional form is derived from exact results in the dilute vapor and hydrodynamic solvent limits. The coefficients A, B, C and D used in modeling high density fluids are determined uniquely from the equation of state of the corresponding hard sphere reference system (33,34)- This hard sphere fluid chemical potential model has been shown to accurately reproduce computer simulation results for both homonuclear and heteronuclear hard sphere diatomics in hard sphere fluids up to the freezing point density (35) ... [Pg.26]

Since in hydrodynamic lubrication the friction force is completely determined by the viscous friction of the lubricant, the coefficient of friction can be calculated from hydrodynamics using the Navier-Stokes equations. This had already been done in 1886 when Reynolds published his classical theory of hydrodynamic lubrication [494], The friction force Fp between two parallel plates of area A separated by the distance d is given by ... [Pg.236]

The set of macroscopic hydrodynamic equations we now deal with, (16), (18)-(20), (27), and (28), follows directly from the initial input in the energy density and the dissipation function without any further assumptions. [Pg.113]

The boundary layer equations may be obtained from the equations provided in Tables 6.1-6.3, with simplification and by an order-of-magnitude study of each term in the equations. It is assumed that the main flow is in the x direction. The terms that are too small are neglected. Consider the momentum and energy equations for the two-dimensional, steady flow of an incompressible fluid with constant properties. The dimensionless equations are given by Eqs. (6.46) to (6.48). The principal assumption made in the boundary layer is that the hydrodynamic boundary layer thickness 8 and the thermal boundaiy layer thickness 8t are small compared to a characteristic dimension L of the body. In mathematical terms,... [Pg.103]


See other pages where From hydrodynamic equations is mentioned: [Pg.686]    [Pg.722]    [Pg.728]    [Pg.24]    [Pg.328]    [Pg.328]    [Pg.185]    [Pg.194]    [Pg.106]    [Pg.151]    [Pg.123]    [Pg.238]    [Pg.296]    [Pg.140]    [Pg.203]    [Pg.702]    [Pg.107]    [Pg.141]    [Pg.75]    [Pg.103]    [Pg.77]   


SEARCH



Hydrodynamic equation

Hydrodynamical equation

© 2024 chempedia.info